(Q36931230)

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Recent advances in the development of recombinant vaccines against classical swine fever virus: cellular responses also play a role in protection

scientific article published on 04 September 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

17 August 2017

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Europe PubMed Central

Recent advances in the development of recombinant vaccines against classical swine fever virus: cellular responses also play a role in protection (English)

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Europe PubMed Central

PubMed publication ID

17 August 2017

classical swine fever

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based on heuristic

inferred from title

classical swine fever virus

object named as

classical swine fever virus

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based on heuristic

inferred from title

Llilianne Ganges

object named as

Llilianne Ganges

1

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Francisco Sobrino

object named as

Francisco Sobrino

3

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Natalia Fernández-Borges

5

object named as

Natalia Fernández-Borges

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Europe PubMed Central

PubMed publication ID

17 August 2017

author name string

José I Núñez

2

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Europe PubMed Central

PubMed publication ID

17 August 2017

Belén Borrego

4

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Europe PubMed Central

PubMed publication ID

17 August 2017

María T Frías-Lepoureau

6

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Europe PubMed Central

PubMed publication ID

17 August 2017

Fernando Rodríguez

7

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Europe PubMed Central

PubMed publication ID

17 August 2017

publication date

4 September 2007

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Europe PubMed Central

PubMed publication ID

17 August 2017

The Veterinary Journal

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Europe PubMed Central

PubMed publication ID

17 August 2017

177

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Europe PubMed Central

PubMed publication ID

17 August 2017

2

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Europe PubMed Central

PubMed publication ID

17 August 2017

169-177

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Europe PubMed Central

PubMed publication ID

17 August 2017

Efficacy of the classical swine fever (CSF) marker vaccine Porcilis Pesti in pregnant sows

1 reference

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Protection of pigs against classical swine fever with DNA-delivered gp55.

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Porcine interleukin-3 enhances DNA vaccination against classical swine fever

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Identification of T-cell epitopes in the structural and non-structural proteins of classical swine fever virus

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Fc gamma RII-dependent sensitisation of natural interferon-producing cells for viral infection and interferon-alpha responses

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Classical swine fever virus induces proinflammatory cytokines and tissue factor expression and inhibits apoptosis and interferon synthesis during the establishment of long-term infection of porcine vascular endothelial cells

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Efficacy and stability of a subunit vaccine based on glycoprotein E2 of classical swine fever virus

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In vitro effect of classical swine fever virus on a porcine aortic endothelial cell line.

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Interaction of classical swine fever virus with dendritic cells.

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Identification of classical swine fever virus protein E2 as a target for cytotoxic T cells by using mRNA-transfected antigen-presenting cells.

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Prevention of transplacental transmission of moderate-virulent classical swine fever virus after single or double vaccination with an E2 subunit vaccine

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Duration of the protection of an E2 subunit marker vaccine against classical swine fever after a single vaccination

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Candidate peptide-vaccines induced immunity against CSFV and identified sequential neutralizing determinants in antigenic domain A of glycoprotein E2.

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Marker vaccine strategies and candidate CSFV marker vaccines

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Candidate multi-peptide-vaccine against classical swine fever virus induced potent immunity with serological marker

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DNA vaccine strategies: candidates for immune modulation and immunization regimens.

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Technical issues in construction of nucleic acid vaccines

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Classical swine fever (CSF) marker vaccine. Trial III. Evaluation of discriminatory ELISAs

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A DNA vaccine expressing the E2 protein of classical swine fever virus elicits T cell responses that can prime for rapid antibody production and confer total protection upon viral challenge.

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Vaccination against classical swine fever virus: limitations and new strategies

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Heterogeneous expression of the non-structural protein p80/p125 in cells infected with different pestiviruses

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Construction of recombinant swinepox viruses and expression of the classical swine fever virus E2 protein

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Vaccination with a single dose of a recombinant porcine adenovirus expressing the classical swine fever virus gp55 (E2) gene protects pigs against classical swine fever

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A prime-boost vaccination strategy using naked DNA followed by recombinant porcine adenovirus protects pigs from classical swine fever

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Classical swine fever virus Strain 'C'. How long is it detectable after oral vaccination?

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Inoculation with DNA encoding the glycoprotein gp2 reduces severity of equine herpesvirus 1 infection in a mouse respiratory model

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Virus antigen expression and alterations in peripheral blood mononuclear cell subpopulations after classical swine fever virus infection

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Targeting plasmid-encoded proteins to the antigen presentation pathways

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Spatial and stochastic simulation to compare two emergency-vaccination strategies with a marker vaccine in the 1997/1998 Dutch Classical Swine Fever epidemic

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Evaluation of genetic vaccine against classical swine fever

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Oronasal vaccination with classical swine fever virus (CSFV) replicon particles with either partial or complete deletion of the E2 gene induces partial protection against lethal challenge with highly virulent CSFV.

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Attenuation of classical swine fever virus by deletion of the viral N(pro) gene

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Introduction to classical swine fever: virus, disease and control policy

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Clinical signs and epidemiology of classical swine fever: a review of new knowledge

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Classical swine fever--an update

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An ELISA detecting antibody to conserved pestivirus epitopes.

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Classical swine fever virus-specific cytotoxic T lymphocytes and identification of a T cell epitope.

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The E2 glycoprotein of classical swine fever virus is a virulence determinant in swine.

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Two overlapping subdominant epitopes identified by DNA immunization induce protective CD8(+) T-cell populations with differing cytolytic activities

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1 reference

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10.1016/J.TVJL.2007.01.030

1 reference

Europe PubMed Central

PubMed publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 August 2017

ResearchGate publication ID

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